MedPath

The Medication Experience Study

Not Applicable
Completed
Conditions
Diabetes
Hypertension
Elevated Cholesterol
Depression
Interventions
Other: Internet Survey
Registration Number
NCT01702883
Lead Sponsor
Wake Forest University
Brief Summary

The purpose of this study is to evaluate whether participation in an Internet-based intervention helps improve medication use.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
186
Inclusion Criteria
  • Any male or female 18 years or older, filling prescriptions for oral medications for hypertension, high cholesterol, diabetes, or depression at the Downtown Health Plaza, Piedmont Plaza, or Cancer Center Pharmacies.
Exclusion Criteria
  • Inability to complete Internet surveys due to inadequate Internet access, not understanding a survey written in English, or lack of computer skills.
  • Patient does not intend to continue using the same WFBMC-affiliated pharmacy for the next 12 months.

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Intervention Group AInternet SurveyRandomization occurs after enrollment survey has been completed. Upon secondary randomization at week eight, this group will continue to receive weekly internet surveys for the entire twelve months. They will be asked to complete the final survey.
Intervention Group CInternet SurveyRandomization occurs after enrollment survey has been completed. This group will complete weekly internet surveys for eight weeks. Upon secondary randomization at week eight, the group will not receive any more internet surveys. They will be asked to complete the final survey.
Intervention Group BInternet SurveyRandomization occurs after enrollment survey has been completed. This group will complete weekly internet surveys for eight weeks. Upon secondary randomization at week eight, this group will begin to receive monthly internet surveys. They will be asked to complete the final survey.
Primary Outcome Measures
NameTimeMethod
The primary measure will be adherence as measured by pharmacy refills in each group.12 months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Wake Forest University Health Sciences

🇺🇸

Winston-Salem, North Carolina, United States

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